MORTON GROVE FDA Approval ANDA 070710

ANDA 070710

MORTON GROVE

FDA Drug Application

Application #070710

Application Sponsors

ANDA 070710MORTON GROVE

Marketing Status

Discontinued001

Application Products

001CONCENTRATE;ORALEQ 2MG BASE/ML0HALOPERIDOLHALOPERIDOL LACTATE

CDER Filings

MORTON GROVE
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70710
            [companyName] => MORTON GROVE
            [docInserts] => ["",""]
            [products] => [{"drugName":"HALOPERIDOL","activeIngredients":"HALOPERIDOL LACTATE","strength":"EQ 2MG BASE\/ML","dosageForm":"CONCENTRATE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"HALOPERIDOL","submission":"HALOPERIDOL LACTATE","actionType":"EQ 2MG BASE\/ML","submissionClassification":"CONCENTRATE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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